Gerandomiseerde studie naar het monitoren van longfunctie bij de opvang van te vroeg geborenen bij de geboorte
Completed
- Conditions
- prematuriteit- prematurityresuscitatie-resuscitation
- Registration Number
- NL-OMON23993
- Lead Sponsor
- eids Universitair Medisch Centrum, Leiden, The Netherlands
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 320
Inclusion Criteria
Infants born will be included in this study if they are between 24 and 27 completed weeks gestation receiving PPV for resuscitation at birth and do not have a known abnormality which might interfere with breathing.
Exclusion Criteria
Infants will be excluded from the final analysis if they are found to have a congenital abnormality or condition that might have an adverse effect on breathing or ventilation, including: congenital diaphragmatic hernia, tracheo-oesophageal fistula or cyanotic heart disease.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The proportion of tidal volumes delivered during manual PPV to an infant within the target range of safe tidal ventilation. The target range of adequate tidal volume is defined as 4-8 mL/kg.
- Secondary Outcome Measures
Name Time Method